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本文引用的文献

1
Formation and function of bacterial organelles.细菌细胞器的形成与功能。
Nat Rev Microbiol. 2020 Dec;18(12):677-689. doi: 10.1038/s41579-020-0413-0. Epub 2020 Jul 24.
2
Decoding the stoichiometric composition and organisation of bacterial metabolosomes.解析细菌代谢体的化学计量组成和结构。
Nat Commun. 2020 Apr 24;11(1):1976. doi: 10.1038/s41467-020-15888-4.
3
Apparent size and morphology of bacterial microcompartments varies with technique.细菌微室的表观大小和形态随技术而变化。
PLoS One. 2020 Mar 9;15(3):e0226395. doi: 10.1371/journal.pone.0226395. eCollection 2020.
4
Encapsulation mechanisms and structural studies of GRM2 bacterial microcompartment particles.GRM2 细菌微隔间颗粒的包封机制和结构研究。
Nat Commun. 2020 Jan 20;11(1):388. doi: 10.1038/s41467-019-14205-y.
5
Bacterial microcompartments: catalysis-enhancing metabolic modules for next generation metabolic and biomedical engineering.细菌微室:用于下一代代谢和生物医学工程的催化增强代谢模块。
BMC Biol. 2019 Oct 10;17(1):79. doi: 10.1186/s12915-019-0691-z.
6
The Plasticity of Molecular Interactions Governs Bacterial Microcompartment Shell Assembly.分子相互作用的可塑性控制着细菌微隔间外壳的组装。
Structure. 2019 May 7;27(5):749-763.e4. doi: 10.1016/j.str.2019.01.017. Epub 2019 Mar 1.
7
Glycyl Radical Enzyme-Associated Microcompartments: Redox-Replete Bacterial Organelles.糖基自由基酶相关微区室:氧化还原态充足的细菌细胞器。
mBio. 2019 Jan 8;10(1):e02327-18. doi: 10.1128/mBio.02327-18.
8
New tools for automated high-resolution cryo-EM structure determination in RELION-3.用于 RELION-3 中自动化高分辨率冷冻电镜结构测定的新工具。
Elife. 2018 Nov 9;7:e42166. doi: 10.7554/eLife.42166.
9
Biotechnological Advances in Bacterial Microcompartment Technology.生物技术在细菌微室技术中的进展。
Trends Biotechnol. 2019 Mar;37(3):325-336. doi: 10.1016/j.tibtech.2018.08.006. Epub 2018 Sep 17.
10
Programmed loading and rapid purification of engineered bacterial microcompartment shells.工程化细菌微室壳的程序化装载和快速纯化。
Nat Commun. 2018 Jul 23;9(1):2881. doi: 10.1038/s41467-018-05162-z.

GRM2细菌微区室颗粒的大小和形态各异。

Variety of size and form of GRM2 bacterial microcompartment particles.

作者信息

Cesle Eva Emilija, Filimonenko Anatolij, Tars Kaspars, Kalnins Gints

机构信息

Structural Biology, Biotechnology and Virusology Laboratory, Latvian Biomedical Research and Study Centre, Riga, Latvia.

CEITEC-Central European Institute of Technology, Masaryk University, Brno, Czech Republic.

出版信息

Protein Sci. 2021 May;30(5):1035-1043. doi: 10.1002/pro.4069. Epub 2021 Apr 2.

DOI:10.1002/pro.4069
PMID:33763934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8040866/
Abstract

Bacterial microcompartments (BMCs) are bacterial organelles involved in enzymatic processes, such as carbon fixation, choline, ethanolamine and propanediol degradation, and others. Formed of a semi-permeable protein shell and an enzymatic core, they can enhance enzyme performance and protect the cell from harmful intermediates. With the ability to encapsulate non-native enzymes, BMCs show high potential for applied use. For this goal, a detailed look into shell form variability is significant to predict shell adaptability. Here we present four novel 3D cryo-EM maps of recombinant Klebsiella pneumoniae GRM2 BMC shell particles with the resolution in range of 9 to 22 Å and nine novel 2D classes corresponding to discrete BMC shell forms. These structures reveal icosahedral, elongated, oblate, multi-layered and polyhedral traits of BMCs, indicating considerable variation in size and form as well as adaptability during shell formation processes.

摘要

细菌微区室(BMCs)是参与酶促过程的细菌细胞器,如碳固定、胆碱、乙醇胺和丙二醇降解等。它们由半透性蛋白质外壳和酶核心组成,能够提高酶的性能并保护细胞免受有害中间体的影响。由于具有封装非天然酶的能力,BMCs在应用方面显示出巨大潜力。为了实现这一目标,详细研究外壳形态的变异性对于预测外壳适应性具有重要意义。在此,我们展示了重组肺炎克雷伯菌GRM2 BMC外壳颗粒的四张新型三维冷冻电镜图,分辨率在9至22埃范围内,以及对应于离散BMC外壳形式的九种新型二维类别。这些结构揭示了BMCs的二十面体、细长、扁球形、多层和多面体特征,表明在外壳形成过程中大小和形态存在相当大的差异以及适应性。